HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 5-Bromo-2-(2-thienylmethoxy)benzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 5-Bromo-2-(2-thienylmethoxy)benzenemethanol | HCID 28981440 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-2-(2-thienylmethoxy)benzyl bromide | HCID 22105505 | — |
Reaction Steps
A solution of 5-bromo-2-(2-thienylmethoxy)benzyl alcohol (0.53 g, 1.77 mmoles) in dichloromethane (12 ml) was cooled in an ice bath and treated with carbon tetrabromide (0.73 g, 2.2 mmol) polymer bound triphenylphosphine (0.65 g, 1.95 mmol) and stirred at ambient temperature for 42 hours. The reaction was filtered and evaporated. Chromatography (eluant: ethyl acetate/hexane) gave 5-bromo-2-(2-thienylmethoxy)benzyl bromide as a white solid (0.29, 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05843942 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-994f6e71f46847b498bd0647c996af81 |
| Source note | uspto-grants-1998_12 |